<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Muller TR</submitter><funding>Deutsches Zentrum für Infektionsforschung</funding><pagination>e1216</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7681835</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(11)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Transgenic re-expression enables unbiased investigation of T-cell receptor (TCR)-intrinsic characteristics detached from its original cellular context. Recent advancements in TCR repertoire sequencing and development of protocols for direct cloning of full TCRαβ constructs now facilitate large-scale transgenic TCR re-expression. Together, this offers unprecedented opportunities for the screening of TCRs for basic research as well as clinical use. However, the functional characterisation of re-expressed TCRs is still a complicated and laborious matter. Here, we propose a Jurkat-based triple parameter TCR signalling reporter endogenous TCR knockout cellular platform (TPR&lt;sup>KO&lt;/sup>) that offers an unbiased, easy read-out of TCR functionality and facilitates high-throughpu</pubmed_abstract><journal>Clinical &amp; translational immunology</journal><pubmed_title>A T-cell reporter platform for high-throughput and reliable investigation of TCR function and biology.</pubmed_title><pmcid>PMC7681835</pmcid><funding_grant_id>FKZ8023807818</funding_grant_id><pubmed_authors>Kohler A</pubmed_authors><pubmed_authors>Leitner J</pubmed_authors><pubmed_authors>Muller TR</pubmed_authors><pubmed_authors>Jutz S</pubmed_authors><pubmed_authors>Schober K</pubmed_authors><pubmed_authors>Busch DH</pubmed_authors><pubmed_authors>Steinberger P</pubmed_authors><pubmed_authors>Schuler C</pubmed_authors><pubmed_authors>Hammel M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A T-cell reporter platform for high-throughput and reliable investigation of TCR function and biology.</name><description>&lt;h4>Objective&lt;/h4>Transgenic re-expression enables unbiased investigation of T-cell receptor (TCR)-intrinsic characteristics detached from its original cellular context. Recent advancements in TCR repertoire sequencing and development of protocols for direct cloning of full TCRαβ constructs now facilitate large-scale transgenic TCR re-expression. Together, this offers unprecedented opportunities for the screening of TCRs for basic research as well as clinical use. However, the functional characterisation of re-expressed TCRs is still a complicated and laborious matter. Here, we propose a Jurkat-based triple parameter TCR signalling reporter endogenous TCR knockout cellular platform (TPR&lt;sup>KO&lt;/sup>) that offers an unbiased, easy read-out of TCR functionality and facilitates high-throughpu</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-19T06:53:44.325Z</modification><creation>2021-02-20T02:52:31Z</creation></dates><accession>S-EPMC7681835</accession><cross_references><pubmed>33251011</pubmed><doi>10.1002/cti2.1216</doi></cross_references></HashMap>